Infrared Irradiation‐Assisted Pd/Cu Catalysis for Sustainable C–N Cross‐Coupling Reactions

Herein, a practical and efficient Pd/Cu‐catalyzed Buchwald–Hartwig amination under infrared irradiation is reported. The reaction proceeds under quasi‐solvent‐free, nonanhydrous conditions and without the need for an inert atmosphere, using only a stoichiometric amount of the green solvent cyclopentyl methyl ether (CPME) as the reaction medium. The cooperative Pd/Cu catalytic system, combined with near‐infrared irradiation centered at 1.2 μm, enables high‐yield C–N couplings of aryl iodides and bromides with a variety of secondary amines with a reduced palladium loading (1.5 mol%) and in short reaction times (1–3 h). Overall, this protocol provides a rapid, sustainable, and broadly applicable route to aryl amines, affording good to excellent yields (68%–99%) under operationally simple conditions.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2026-07-26
DOI
https://doi.org/10.1002/ejoc.70714
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
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article

Infrared Irradiation‐Assisted Pd/Cu Catalysis for Sustainable C–N Cross‐Coupling Reactions

Gianluca M. Farinola, Ambra Maria Fiore, Angela Punzi, Pietro Cotugno et al.
European Journal of Organic Chemistry
Catalytic Cross-Coupling Reactions
article

Infrared Irradiation‐Assisted Pd/Cu Catalysis for Sustainable C–N Cross‐Coupling Reactions

Gianluca M. Farinola, Ambra Maria Fiore, Angela Punzi, Pietro Cotugno, Matteo R. Martina
article en

Abstract

Herein, a practical and efficient Pd/Cu‐catalyzed Buchwald–Hartwig amination under infrared irradiation is reported. The reaction proceeds under quasi‐solvent‐free, nonanhydrous conditions and without the need for an inert atmosphere, using only a stoichiometric amount of the green solvent cyclopentyl methyl ether (CPME) as the reaction medium. The cooperative Pd/Cu catalytic system, combined with near‐infrared irradiation centered at 1.2 μm, enables high‐yield C–N couplings of aryl iodides and bromides with a variety of secondary amines with a reduced palladium loading (1.5 mol%) and in short reaction times (1–3 h). Overall, this protocol provides a rapid, sustainable, and broadly applicable route to aryl amines, affording good to excellent yields (68%–99%) under operationally simple conditions.

European Journal of Organic Chemistry
University of Bari Aldo Moro (IT)
Responsible consumption and production
Openalex Percentile: Top 16%
Catalytic Cross-Coupling Reactions
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